Our Standard
What has to be true
before it reaches you.
Every Omnivia formulation clears the same requirements before it reaches you — what goes into it, how it is made, how it is tested. Nothing here is optional, and nothing here is negotiable.
01 — Sourcing
Traced to the farm,
not to the broker.
The supplement industry runs on commodity brokerage. A botanical can pass through several intermediaries between the field and the finished capsule, and at each transfer the documentation grows thinner. Most brands never ask what happened in between.
We ask. Before a product joins the collection we look at what is actually in it, at what quantity, and whether that quantity resembles anything the published research would recognize. Where a formulation cannot clear that bar, we do not list it — which is why this collection is small.
Standardized, not
merely weighed.
Five hundred milligrams of a botanical extract tells you nothing. Five hundred milligrams standardized to a specified percentage of its active constituent tells you what you are actually taking. Every botanical in our line carries a standardization specification, and every incoming lot is assayed against it before acceptance.
FDA-registered manufacturing under 21 CFR Part 111.
02 — Manufacturing
Made in the United States,
under a standard with teeth.
Every Omnivia product is manufactured in the United States, in FDA-registered facilities operating under the dietary-supplement cGMP rules in 21 CFR Part 111.
What sets the bar higher is how much we require before agreeing to list anything: the manufacturing standard behind the plant, and the independent testing behind the formulation. We ask for both, every time, and we decline more than we accept.
FDA-registered facilities
Subject to inspection, operating under current Good Manufacturing Practice.
Documented, not just asserted
We ask for the paperwork, and we read it before we list a product.
Tested before we list it
Reviewed before a product joins the collection.
Dedicated allergen protocols
Segregated lines and validated cleaning between runs.
03 — Testing
Four assays, independently run.
Identity
Manufacturers verify that incoming material matches its specification before it enters production, under the identity-testing requirements of 21 CFR Part 111.
Required under 21 CFR 111
Potency
Finished-product testing confirms the active constituent against the label claim.
Tested, not asserted
Contaminants
Heavy metals, pesticide residues, residual solvents and microbial load, screened against specification limits.
Screened, not assumed
Stability
Manufacturers establish shelf life through stability testing, which is what the expiry date on your carton represents.
Behind the expiry date
04 — Transparency
Every active, named.
Not one.
Every ingredient in every Omnivia formulation is named on the label. Not a category, not a gesture — the actual botanical, the actual compound, the actual form it takes.
Where a formulation carries a traditional blend, we say so plainly and we name everything inside it. What we will not do is put something on the front of a carton that you cannot find on the back.
Tested independently
before it ships.
Every formulation in this collection is independently tested for composition and contaminants before it reaches you. That testing is not a favor we do on request — it is a condition of the product existing at all. It happens on every batch, whether anyone asks or not.
What that buys you is simple: when the label says a dose, that is the dose in the bottle.
What we will not do. We will not make disease claims. We will not cite an animal study as though it were human evidence. We will not describe an ingredient trial as a product trial. We will not put a celebrity where a citation belongs. And we will not add an ingredient because it tests well in a focus group when the research does not support it.
Because most of the cost sits in places you cannot see on a shelf. Identity testing every incoming lot. Independent finished-product assay. Standardized extracts rather than crude powder. Doses matched to trials rather than to margin. Stability programs that hold the label claim to expiry.
A capsule that costs eight cents to fill and a capsule that costs fifty look identical. The difference only becomes visible in an assay — which is precisely why we publish ours.
It varies by formulation and is stated explicitly on each product page under 'Free from'. Several products — Colostrum Powder most obviously — are dairy-derived and cannot be vegan. We would rather be accurate about that than apply a blanket claim that is true for some of our line and false for the rest.
No artificial colors or flavours, and no titanium dioxide. Where a flow agent is genuinely required for encapsulation we use the minimum quantity of an inert, food-grade material and disclose it on the label. We do not pretend that manufacturing at scale requires nothing but the actives — but we do keep the list as short as the process allows.
The lot is quarantined and does not ship. Depending on the failure mode it is either reworked under documented procedure or destroyed. We investigate root cause with the supplier, and a repeated failure ends the relationship. This has happened. It will happen again. The system working means occasionally absorbing the cost of material we cannot sell.